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Clinical Trials/RPCEC00000408
RPCEC00000408Completed未知

Immunogenicity evaluation of the heterologous combination of two doses of SINOPHARM and one dose of SOBERANA Plus: a post-authorization study for emergency use (COVID-19) - Sinopharm-SOBERANA COVID-Cienfuegos

Finlay Vaccine Institute0 sites202 target enrollmentStarted: August 30, 2022Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Enrollment
202

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
N/a: Single Arm Study. Masking: Open. Control Group: Uncontrolled. Assignment: Single Group. Purpose: Prevention

Eligibility Criteria

Ages
19 years to none (—)
Sex
All

Inclusion Criteria

  • 1.- Subjects with 19 years or more, who were eligible for vaccination with SINOPHARM and SOBERANA Plus in the province of Cienfuegos.
  • 2.- Subjects who give informed consent for blood extraction at the scheduled times.

Exclusion Criteria

  • 1.- Pregnancy, puerperium or lactation.
  • 2.- Subjects with a history of having suffered from COVID-19

Investigators

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